Real-time focusing in line scan imaging

ABSTRACT

Systems and methods for capturing a digital image of a slide using an imaging line sensor and a focusing line sensor. In an embodiment, a beam-splitter is optically coupled to an objective lens and configured to receive one or more images of a portion of a sample through the objective lens. The beam-splitter simultaneously provides a first portion of the one or more images to the focusing sensor and a second portion of the one or more images to the imaging sensor. A processor controls the stage and/or objective lens such that each portion of the one or more images is received by the focusing sensor prior to it being received by the imaging sensor. In this manner, a focus of the objective lens can be controlled using data received from the focusing sensor prior to capturing an image of a portion of the sample using the imaging sensor.

CROSS REFERENCING TO RELATED APPLICATIONS

The present application is a continuation of U.S. patent applicationSer. No. 16/224,397, filed on Dec. 18, 2018, which is a continuation ofU.S. patent application Ser. No. 15/838,043, filed on Dec. 11, 2017,which is a continuation of U.S. patent application Ser. No. 14/398,443,filed on Oct. 31, 2014, which is a national stage entry of InternationalPatent App. No. PCT/US2013/031045, filed on Mar. 13, 2013, which claimspriority to U.S. Provisional App. No. 61/641,788, filed on May 2, 2012,each of which is incorporated herein by reference as if set forth infull.

BACKGROUND Field of the Invention

The present invention generally relates to digital pathology and moreparticularly relates to a multiple independent linear sensor apparatusfor performing real-time focusing in line scan imaging.

Related Art

Most auto-focus methods in microscopic imaging systems can be dividedinto two categories: laser-based interferometer for sensing slideposition and image content analysis. The image content analysis methodsrequire multiple image acquisitions at different focus depths and usealgorithms to compare the images to determine the best focus. Acquiringthe multiple images may create time delays between focusing and imaging.Measuring the reflection of the laser beam off a slide surface canprovide only global focus information of the slide or the cover slipposition. It lacks focusing accuracy to tissues with large heightvariations.

Therefore, what is needed is a system and method that overcomes thesesignificant problems found in the conventional systems as describedabove.

SUMMARY

In an embodiment, the present invention is based on image contentanalysis (e.g., tissue finding and macro focus), and takes advantage ofline imaging and line focusing for accurate real-time auto-focusing,without having to take multiple images for focusing which wouldintroduce a time delay during scanning. In one embodiment, full stripefocusing is performed during a retrace process of line scanning. In analternative embodiment, focusing is performed during image scanning.Both embodiments eliminate time delays in image scanning, thus speedingup the entire digital image scanning process.

In an embodiment, a system for capturing a digital image of a slide isdisclosed. The system comprises an objective lens having a singleoptical axis; a motorized positioner to control the objective lens; astage configured to support a sample; at least one imaging sensor; atleast one focusing sensor; at least one beam-splitter optically coupledto the objective lens and configured to receive one or more images of atleast a portion of the sample through the objective lens, andsimultaneously provide a first portion of the one or more images to theat least one focusing sensor and a second portion of the one or moreimages to the at least one imaging sensor; and at least one processorthat controls one or more of the stage and the objective lens such thateach portion of the one or more images is received by the at least onefocusing sensor prior to it being received by the at least one imagingsensor.

In a further embodiment, a method for capturing a digital image of aslide is disclosed. The method comprises, by an objective lens having asingle optical axis, acquiring one or more images of at least a portionof a sample supported on a stage; by at least one beam-splitteroptically coupled to the objective lens, simultaneously providing afirst portion of the one or more images to at least one focusing sensorand a second portion of the one or more images to at least one imagingsensor; and by at least one processor, controlling one or more of thestage and the objective lens such that each portion of the one or moreimages is received by the at least one focusing sensor prior to it beingreceived by the at least one imaging sensor.

In an additional embodiment, a system for capturing a digital image of aslide is disclosed. The system comprises an objective lens; a stageconfigured to support a sample; at least one imaging sensor comprising alinear array and a wedge prism, the linear array configured to receive alight path via the objective lens; at least one processor that controlsthe wedge prism by moving the wedge prism into the light path during aretrace operation and moving the wedge prism out of the light pathduring a scan operation, receives digital image data from a retraceoperation of at least a portion of the sample, determines a focus heightbased on the digital image data, and adjusts the height of the objectivelens to the focus height prior to a scan operation of the at least aportion of the sample.

Other features and advantages of the present invention will become morereadily apparent to those of ordinary skill in the art after reviewingthe following detailed description and accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The structure and operation of the present invention will be understoodfrom a review of the following detailed description and the accompanyingdrawings in which like reference numerals refer to like parts and inwhich:

FIG. 1 is a block diagram illustrating an example side viewconfiguration of a scanning system, according to an embodiment;

FIG. 2 is a block diagram illustrating an example configuration of afocusing sensor and imaging sensor with respect to a radius ofillumination and a circular optical field of view, according to anembodiment;

FIG. 3A is a block diagram illustrating an example top viewconfiguration of a imaging sensor, according to an embodiment;

FIG. 3B is a block diagram illustrating an example top viewconfiguration of a focusing sensor, according to an embodiment;

FIG. 4 is a block diagram illustrating an example focusing sensor,according to an embodiment;

FIG. 5 is a time chart diagram illustrating an example interplay betweena focusing sensor and an imaging sensor during scanning, according to anembodiment;

FIG. 6 is a block diagram illustrating an example non-tilted focusingsensor with a prism, according to an embodiment;

FIGS. 7A and 7B are block diagrams illustrating an example dual imagingand focusing sensor with a moveable prism, according to an embodiment;

FIG. 8 is a block diagram illustrating an example multiple focusingsensor configuration of a scanning system, according to an embodiment;

FIG. 9 is a block diagram illustrating an example slide motion of ascanning system, according to an embodiment;

FIG. 10 is a block diagram illustrating an example focusing sensor witha microlens array, according to an embodiment;

FIG. 11 is a block diagram illustrating an example non-tilted focusingsensor with a microlens array and a prism, according to an embodiment;

FIG. 12A is a block diagram illustrating an example microscope slidescanner, according to an embodiment;

FIG. 12B is a block diagram illustrating an alternative examplemicroscope slide scanner, according to an embodiment;

FIG. 12C is a block diagram illustrating example linear sensor arrays,according to an embodiment; and

FIG. 13 is a block diagram illustrating an example wired or wirelessprocessor-enabled device that may be used in connection with variousembodiments described herein.

DETAILED DESCRIPTION

Certain embodiments disclosed herein provide for real-time (i.e.,instantaneous or near-instantaneous) focusing in line scan imaging usingmultiple linear detectors or other components. After reading thisdescription it will become apparent to one skilled in the art how toimplement the invention in various alternative embodiments andalternative applications. However, although various embodiments of thepresent invention will be described herein, it is understood that theseembodiments are presented by way of example only, and not limitation. Assuch, this detailed description of various alternative embodimentsshould not be construed to limit the scope or breadth of the presentinvention as set forth in the appended claims.

FIG. 1 is a block diagram illustrating an example side viewconfiguration of a scanning system 10, according to an embodiment. Inthe illustrated embodiment, the scanning system 10 comprises a tissueslide 120 that is placed on a motorized stage (not shown) andilluminated by an illumination system (not shown) and moved in ascanning direction 65. An objective lens 130 has an optical field ofview that is trained on the slide 120 and provides an optical path forlight from the illumination system that passes through the specimen onthe slide or reflects off of the specimen on the slide or fluorescesfrom the specimen on the slide or otherwise passes through the objectivelens 130. The light travels on the optical path to a beam splitter 140that allows some of the light to pass through lens 160 to an imagingsensor 20. The light may optionally be bent by a mirror 150 as shown inthe illustrated embodiment. The imaging sensor 20 may be, for example, aline charge-coupled device (CCD).

Other of the light travels from the beam splitter 140 through lens 165to a focusing sensor 30. The focusing sensor 30 may also be, forexample, a line charge-coupled device (CCD). The light that travels tothe imaging sensor 20 and the focusing sensor 30 preferably representsthe complete optical field of view from the object lens 130. Based onthe configuration of the system, the scanning direction 65 of the slide120 is logically oriented with respect to the imaging sensor 20 and thefocusing sensor 30 so that the logical scanning direction 60 causes theoptical field of view of the objective lens 130 to pass over therespective imaging sensor 20 and focusing sensor 20.

As shown in the illustrated embodiment, the imaging sensor 20 iscentered within the optical field of view of the objective lens 130while the focusing sensor 30 is shifted away from the center of theoptical field of view of the objective lens 130. The direction in whichthe focusing sensor 30 is shifted away from the center of the opticalfield of view of the objective lens 130 is the opposite of the logicalscanning direction 60. This placement logically orients the focusingsensor 30 in front of the imaging sensor 20 such that as a specimen on aslide is scanned, the focusing sensor 30 “sees” the image data beforethe imaging sensor 20 “sees” that same image data. Finally, the focusingsensor 30 is tilted within the optical field of view such that lightfrom the objective is sensed by the focusing sensor 30 at a plurality ofZ values.

FIG. 2 is a block diagram illustrating an example configuration of afocusing sensor 30 and imaging sensor 20 with respect to a circularillumination radius 40 and an optical field of view 50, according to anembodiment. In the illustrated embodiment, the positioning of thefocusing sensor 30 is shown with respect to the imaging sensor 20 andthe logical scan direction 60. The scan direction 60 in this case,refers to the direction in which the stage or specimen (e.g., a tissuesample) is moving with respect to the sensors 20 and 30 in space. Asillustrated, the sample will reach the focusing sensor 30 first, and theimaging sensor 20 second. When the imaging sensor 20 and the focusingsensor 30 are projected onto a same plane using, for example abeam-splitter, the focusing sensor 30 is within the illumination circle,which has a radius R, of the optical field of view 50 at a locationahead of the primary imaging sensor 20 in terms of the logical scanningdirection 60. Thus, when a section of a tissue sample passes thefocusing sensor 30, focus data can be captured and the focus heightcalculated based on one or more predetermined algorithms. The focus dataand focus height can be used to control (e.g., by a controller) thedistance between an objective lens height and the tissue sample beforethe same section of the tissue sample is sensed by the primary imagingsensor 20 via the same objective.

The circular illumination radius 40 preferably illuminates an opticalfield of view 50 (FOV) covering both the focusing sensor 30 and theimaging sensor 20. The radius R is a function of the FOV on the objector sample and the optical magnification of the focusing optical pathM_(focusing). The function can be expressed as:2R=FOV*M _(focusing)

For M_(focusing)=20 and FOV=1.325 mm (e.g., Olympus PlanApo 20×objective), R=13.25 mm. The imaging sensor 20 is projected in the middleof the optical field of view 50 for best image quality, while thefocusing sensor 30 is located off-center with respect to the opticalfield of view 50 by a distance h from the imaging sensor 20. There is arelationship among the distance h, the radius R, and the focusing sensor30 length L, such that:h≤square root(R ²−(L/2)²)for a sensor length=20.48 mm and R=13.25 mm, h≤8.4 mm.

The available time t for the focusing sensor 30 to capture multiplecamera lines, for focus height calculation and for moving the objectiveto the right Z value height, is a function of the distance h between thefocusing sensor 30 and the imaging sensor 20, magnificationM_(focusing), and scan speed v:v*t=h/M _(focusing)

For a scan speed of 4.6 mm/s, the maximum time available is about 91.4ms for M_(focusing)=20 and h=8.4 mm. The maximum number of camera linescaptured by the focusing sensor 30, available for the focus calculationis:

N=t*κ, where □ is the line rate of the focusing sensor 30.

For a camera line rate of 18.7 kHz, N_(max)=1,709 lines, where theobjective stays at the same height. Otherwise, N<N_(max) to allow theobjective to move to the next focus height.

At a high level, a tissue sample is passed under an objective lens in anX direction. A portion of the tissue sample is illuminated to create anilluminated view in the Z direction of a portion of the sample. Theilluminated view passes through the objective lens which is opticallycoupled to both the focusing sensor 30 and imaging sensor 20, forexample, using a beam splitter. The focusing sensor 30 and imagingsensor 20 are positioned such that the focusing sensor 30 receives aportion or line of the view before the imaging sensor 20 receives thesame portion or line. In other words, as the focusing sensor 30 isreceiving a first line of image data, the imaging sensor 20 issimultaneously receiving a second line of image data which waspreviously received by the focusing sensor 30 and which is a distanceh/M_(focusing) on the sample from the first line of image data. It willtake a time period Δt for the imaging sensor 20 to receive the firstline of image data after the focusing sensor 30 has received the firstline of image data, where Δt represents the time that it takes thesample to move a distance h/M_(focusing) in the scan direction.

During that period Δt, a processor of the scanning system 10 calculatesan optimal focus height in the Z direction for the first line of imagedata, and adjusts the objective lens to the calculated optimal focusheight. For instance, in an embodiment, the focusing sensor 30 isseparate from the imaging sensor 20 and is tilted at an angle θ withrespect to a direction that is perpendicular to the optical imagingpath. Thus, the focusing sensor 30 receives pixels of image data at aplurality of Z values. The processor may then determine which Z heightvalue corresponds to the pixel(s) of image data having the best focus(e.g., having the highest contrast with respect to the other pixels).After the optimal Z height value is determined, the processor or othercontroller may move the objective lens in the Z direction to thedetermined optimal Z height value before or simultaneously with theimaging sensor receiving the first line of image data.

FIG. 3A is a block diagram illustrating an example top viewconfiguration of a imaging sensor 20 with respect to an imaging opticalpath 210, according to an embodiment. Similarly, FIG. 3B is a blockdiagram illustrating an example top view configuration of a focusingsensor 30, with respect to a focusing optical path 200, according to anembodiment. As can be seen in FIG. 3B, the focusing sensor 30 is tiltedat an angle θ with respect to a direction that is perpendicular to thefocusing optical path 200.

FIG. 4 is a block diagram illustrating an example focusing sensor 30,according to an embodiment. In the illustrated embodiment, within arange of focusing (z) on a tissue sample (e.g., 20 □m), the focusingsensor 30 comprises a plurality of sensor pixels 218 and may bepositioned at a location where the entire focusing range (z) in the Zdirection is transferred by optics to the entire focusing sensor 30array in the Y direction (orthogonal to the X direction, i.e., scandirection), as shown. The sensor pixel 218 location is directlycorrelated to the Z position of the objective at focus. As illustratedin FIG. 4, each dashed line, p₁, p₂, . . . p_(i) . . . p_(n), acrossprojected focusing range (d) represents a different focus value andcorresponds to a focus height, i.e., Z height, of the objective lens.The p_(i) having the optimal focus for a given portion of a sample canbe used by the scanning system to determine the optimal focus height forthat portion of the sample.

The relationship between the projected focusing range (d) on thefocusing sensor 30 and the focusing range (z) on the specimen object isas follows:

d=z*M_(focusing) ², where M_(focusing) is the optical magnification ofthe focusing path. For instance, if z=20 □m and M_(focusing)=20, thend=8 mm.

In order to cover the entire projected focusing range (d) by a tiltedfocusing sensor 30 that is a linear array sensor, the tilting angle □should follow the relationship:

sin □=d/L, where L is the length of the sensor 30.

Using d=8 mm and L=20.48 mm, □=23.0°. □□ and L can vary as long as thetilted sensor 30 covers the entire focusing range (z).

The focusing resolution, or the minimum step of objective height motion□z is a function of the sensor pixel size, e=minimum(□L). Derived fromthe above formulas:□z=e*z/L.

For instance, if e=10 □m, L=20.48 mm, and z=20 □m, then □z=0.0097 □m<10nm.

In an embodiment, one-dimensional data from the focusing sensor 30 isanalyzed. A figure of merit (FOM) (e.g., contrast of the data) may bedefined. The pixel 218 location (Z value) of the maximum FOM on thesensor array can be found. In this manner, the focus position (Z value)of the objective can be determined for that scan line on the sample.

The relationship between the objective height Z_(i) and the focuslocation L_(i) on the focusing sensor of focus point i is:L _(i) =Z _(i) *M _(focusing) ²/sin □

If the focus height is determined by a mean from L₁ to L₂, according tothe analysis of the data from the focusing sensor 30 discussed above,the objective height needs to be moved from Z₁ to Z₂ based on:Z ₂ =Z ₁+(L ₂ −L ₁)*sin □/M _(focusing) ²

Although the field of view (FOV) in the Y axis of the focusing sensor 30and the imaging sensor 20 can be different, the centers of both sensorsare preferably aligned to each other along the Y axis.

FIG. 5 is a time chart diagram illustrating an example interplay betweena focusing sensor 30 and an imaging sensor 20 during scanning, accordingto an embodiment. In the illustrated embodiment, the timing of a scanusing an imaging sensor 30 and focusing sensor 20 is shown. At time t₀,the Z position of the objective lens is at height Z₀ on tissue sectionX₁, which is in the field of view of the focusing sensor 30. Thefocusing sensor 30 receives focusing data corresponding to tissuesection X₁. The focus height Z₁ is determined to be the optimal focusheight for tissue section X₁ using the focusing data and, in someembodiments, associated focusing algorithms. The optimal focus height isthen fed to the Z positioner to move the objective lens to the heightZ₁, for example, using a control loop. At t₁, tissue section X₁ is movedinto the field of view of the imaging sensor 20. With the correct focusheight, the imaging sensor 20 will sense an optimally focused image ofthe sample. At the same time t₁, the focusing sensor 30 capturesfocusing data from tissue section X₂, and the focusing data will be usedto determine the optimal focus height Z₂ which in turn will be fed intothe Z positioner prior to or at the time that tissue section X₂ passesinto the field of view of the imaging sensor 20 at time t₂. Such aprocess can continue until the entire tissue sample is scanned.

In general at time t_(n), tissue section X_(n+1) is in the field of viewof the focusing sensor, tissue section X_(n) is in the field of view ofthe imaging sensor 30, and the objective lens is at a Z height of Z_(n).Furthermore, prior to or at the time t_(n+1), the optimal focus heightfor tissue section X_(n+1) is determined and the Z height of theobjective lens is adjusted to Z_(n+1). Considering FIG. 2, at time t₀,the focusing sensor 30 “sees” tissue section X₁ and determines the focusheight as Z₁ for tissue section X₁; at time t₁, tissue section X₁ movesunder the imaging sensor 20 and the objective moves to height Z₁ whilethe focusing sensor 30 “sees” tissue section X₂ and determines the focusheight as Z₂ for tissue section X₂; at time t_(n), tissue section X_(n)moves under the imaging sensor 20 and the objective moves to heightZ_(n) while the focusing sensor 30 “sees” tissue section X_(n+1) anddetermines the focus height as Z_(n+1) for tissue section X_(n+1). Aperson of skill in the art should understand that X_(n−1) and X_(n) donot necessarily represent consecutive or adjacent lines of image data,as long as a scan line is acquired by the focusing sensor 30 and anoptimal focus height for the scan line is determined and set prior tothe same scan line being acquired by the imaging sensor 20. In otherwords, the focusing sensor 30 and imaging sensor 20 may be arranged suchthat one or more scan lines exist between the focusing sensor's 30 fieldof view and the imaging sensor's 20 field of view, i.e., that distance hbetween the focusing sensor 30 and imaging sensor 20 comprises one ormore scan lines of data. For instance, in that case that the distance hcomprises 5 scan lines, tissue section X₆ would be in the field of viewof the focusing sensor 30 at the same time that tissue section X₁ is inthe field of view of the imaging sensor 20. In this case, the focusheight of the objective lens would be adjusted to the calculated optimalfocus height after the tissue section X₅ is sensed by the imaging sensor20 but prior to the tissue section X₆ being sensed by the imaging sensor20. Advantageously, the focus height of the objective lens may besmoothly controlled between tissue section X₁ and X₆ such that there areincremental changes in focus height between X₁ and X₆ that approximate agradual slope of the tissue sample.

FIG. 6 is a block diagram illustrating an example non-tilted focusingsensor 30 with a prism 270, according to an embodiment. In theillustrated embodiment, FIG. 6 shows an alternative to the tiltedfocusing line sensor 30. Instead of tilting the focusing sensor 30, awedge prism 270 attached to the focusing sensor 30 can be used toperform a similar focusing function. Alternatively, a combination of awedge prism 270 and a tilted focusing sensor 30 could be employed. Thealgorithms and procedure may remain the same in such an alternativeembodiment. Furthermore, if two parallel linear sensor arrays withsufficient spacing between the sensors can be integrated into a singlefield of view, a wedge prism 270 can be attached onto the focusingsensor 30 for focusing and the imaging sensor 20 can be used for sensingimage data from the sample.

FIGS. 7A and 7B are block diagrams illustrating an example dual imagingand focusing sensor with a moveable prism, according to an embodiment.Advantageously, in this embodiment the same physical sensor can be usedas both the focusing sensor 30 and the imaging sensor 20. As shown inFIG. 7A, when the wedge prism 270 is in place, the sensor performs thefunctions of the focusing sensor 30. The wedge prism 270 is in placewhen the wedge prism 270 is placed within the field of view of at leasta portion of the sensor. Correspondingly, when the wedge prism 270 isnot in place, the sensor performs the functions of the imaging sensor20. The wedge prism 270 is not in place when no portion of the wedgeprism 270 is within the field of view of the sensor.

Such an embodiment can be used in connection with a scanning motion suchas the motion described with respect to FIG. 9 whereby the scanningsystem focuses during a first pass of the sample under the objectivelens and then the scanning system images during a second pass of thesame portion of the sample under the objective lens. During the firstpass, the wedge prism 270 is in place and during the second pass, thewedge prism 270 is not in place.

FIG. 8 is a block diagram illustrating an example multiple focusingsensor configuration of a scanning system, according to an embodiment.In the illustrated embodiment, the scanning system employs at least twofocusing sensors 30 and 35. In the illustrated embodiment, the secondfocusing sensor 35 may comprise a linear sensory array tilted in theopposite direction as the first focusing sensor 30. The second focusingsensor 35 can perform the same focusing function as the first focusingsensor 30 to allow the scanning system to analyze data obtained from thetwo focusing sensors 30 and 35 and calculate a more precise optimalfocus height for the objective lens when the imaging sensor passes overthe specimen. For example, the scanning system may use the dual focusingsensor 30 35 data for averaging or compensation. The second focusingsensor 35 may be the third linear sensor array of the scanning system,when combined with the first focusing sensor 30 and the primary imagingsensor 20.

FIG. 10 is a block diagram illustrating an example focusing sensor 30with a microlens array 250, according to an embodiment. In theillustrated embodiment, a linear microlens array 250 (tilted ornon-tilted) is positioned in the FOV of the tilted focusing sensor 30(e.g., a linear sensor array) to have multiple micro images of anidentical tissue section. This embodiment can be used to avoid possibleambiguity associated with partial tissue within the FOV, which mayresult from previously described embodiments and methods. In oneembodiment, the minimum dimension of the microlens array 250 is to coverthe cross-section of the light path falling onto the focusing sensor 30,whether the microlens array 250 is either tilted or not tilted. Thenumber of microlens array 250 elements is determined by the Z resolutionand the total focusing range. For instance, if a 0.5 □m resolution isrequired over a 20 □m focusing range, the number of lens elements is 40.

In one embodiment, the field lens 260 is used to reduce the vignettingeffect in the scanning system and does not impact system magnification.In a microlens array 250 embodiment, the method to determine the bestfocus may be different than the figure of merit technique describedabove. For example, the scanning system may compare the averagecontrast, for example, among 40 microlens images with a 0.5 □m depthincrement. The center location of the highest contrast in the image isfound and the objective height is then determined based on the sameformula as discussed above: L_(i)=Z_(i)*M_(focusing) ²/sin □.

FIG. 11 is a block diagram illustrating an example non-tilted focusingsensor 30 with a microlens array 250 and a prism 270, according to anembodiment. In the illustrated embodiment, the microlens array 250 isintegrated with a wedge prism 270 in front of the focusing sensor 30(e.g., a line sensor) to perform the focusing function.

FIGS. 12A and 12B are block diagrams illustrating example microscopeslide scanners, according to an embodiment and FIG. 12C is a blockdiagram illustrating example linear sensor arrays, according to anembodiment. These three figures will be described in more detail below,however they will first be described in combination to provide anoverview. It should be noted that the following description is just anexample of a slide scanner device and that alternative slide scannerdevices can also be employed. FIGS. 12A and 12B illustrate examplemicroscope slide scanners that can be used in conjunction with thedisclosed sensor arrangement. FIG. 12C illustrates example linearsensors, which can be used in any combination as the disclosed sensors(imaging sensors or focusing sensors).

For example, the imaging sensor and the focusing sensor(s) may bearranged (e.g., in conjunction with a beam-splitter), as discussedabove, using line scan camera 18 as the primary imaging sensor andfocusing sensor 20 as the focusing sensor in combination with the beamsplitter 140. In one embodiment, the line scan camera 18 may includeboth the focusing sensor and the primary imaging sensor. The imagingsensor and focusing sensor(s) can receive image information from asample 12 through the microscope objective lens 16 and/or the focusingoptics 34 and 290. Furthermore, they can provide information to, and/orreceive information from, data processor 21. Data processor 21 iscommunicatively connected to memory 36 and data storage 38. Dataprocessor 21 may further be communicatively connected to acommunications port, which may be connected by at least one network 42to one or more computers 44, which may in turn be connected to displaymonitor(s) 46.

Data processor 21 may also be communicatively connected to and provideinstructions to a stage controller 22, which controls a motorized stage14 of the slide scanner 11. The motorized stage 14 supports sample 12and moves in one or more directions in the X-Y plane. In one embodiment,the motorized stage 14 may also move in the Z plane. Data processor 21may also be communicatively connected to and provide instructions to amotorized controller 26, which controls a motorized positioner 24 (e.g.,a piezo positioner). The motorized positioner 24 is configured to movethe objective lens 16 in the Z direction. The slide scanner 11 alsocomprises a light source 31 and/or illumination optics 32 to illuminatethe sample 12, either from above or below.

Turning now to FIG. 12A, a block diagram of an embodiment of an opticalmicroscopy system 10 according to the present invention is shown. Theheart of the system 10 is a microscope slide scanner 11 that serves toscan and digitize a specimen or sample 12. The sample 12 can be anythingthat may be interrogated by optical microscopy. For instance, the sample12 may be a microscope slide or other sample type that may beinterrogated by optical microscopy. A microscope slide is frequentlyused as a viewing substrate for specimens that include tissues andcells, chromosomes, DNA, protein, blood, bone marrow, urine, bacteria,beads, biopsy materials, or any other type of biological material orsubstance that is either dead or alive, stained or unstained, labeled orunlabeled. The sample 12 may also be an array of any type of DNA orDNA-related material such as cDNA or RNA or protein that is deposited onany type of slide or other substrate, including any and all samplescommonly known as a microarrays. The sample 12 may be a microtiterplate, for example a 96-well plate. Other examples of the sample 12include integrated circuit boards, electrophoresis records, petridishes, film, semiconductor materials, forensic materials, or machinedparts.

The scanner 11 includes a motorized stage 14, a microscope objectivelens 16, a line scan camera 18, and a data processor 21. The sample 12is positioned on the motorized stage 14 for scanning. The motorizedstage 14 is connected to a stage controller 22 which is connected inturn to the data processor 21. The data processor 21 determines theposition of the sample 12 on the motorized stage 14 via the stagecontroller 22. In one embodiment, the motorized stage 14 moves thesample 12 in at least the two axes (x/y) that are in the plane of thesample 12. Fine movements of the sample 12 along the optical z-axis mayalso be necessary for certain applications of the scanner 11, forexample, for focus control. Z-axis movement is preferably accomplishedwith a piezo positioner 24, such as the PIFOC from Polytec PI or theMIPOS 3 from Piezosystem Jena. The piezo positioner 24 is attacheddirectly to the microscope objective 16 and is connected to and directedby the data processor 21 via a piezo controller 26. A means of providinga coarse focus adjustment may also be needed and can be provided byz-axis movement as part of the motorized stage 14 or a manualrack-and-pinion coarse focus adjustment (not shown).

In one embodiment, the motorized stage 14 includes a high precisionpositioning table with ball bearing linear ways to provide smooth motionand excellent straight line and flatness accuracy. For example, themotorized stage 14 could include two Daedal model 106004 tables stackedone on top of the other. Other types of motorized stages 14 are alsosuitable for the scanner 11, including stacked single axis stages basedon ways other than ball bearings, single- or multiple-axis positioningstages that are open in the center and are particularly suitable fortrans-illumination from below the sample, or larger stages that cansupport a plurality of samples. In one embodiment, motorized stage 14includes two stacked single-axis positioning tables, each coupled to twomillimeter lead-screws and Nema-23 stepping motors. At the maximum leadscrew speed of twenty-five revolutions per second, the maximum speed ofthe sample 12 on the motorized stage 14 is fifty millimeters per second.Selection of a lead screw with larger diameter, for example fivemillimeters, can increase the maximum speed to more than 100 millimetersper second. The motorized stage 14 can be equipped with mechanical oroptical position encoders which has the disadvantage of addingsignificant expense to the system. Consequently, such an embodiment doesnot include position encoders. However, if one were to use servo motorsin place of stepping motors, then one would have to use positionfeedback for proper control.

Position commands from the data processor 21 are converted to motorcurrent or voltage commands in the stage controller 22. In oneembodiment, the stage controller 22 includes a 2-axis servo/steppermotor controller (Compumotor 6K2) and two 4-amp microstepping drives(Compumotor OEMZL4). Microstepping provides a means for commanding thestepper motor in much smaller increments than the relatively largesingle 1.8 degree motor step. For example, at a microstep of 100, thesample 12 can be commanded to move at steps as small as 0.1 micrometer.A microstep of 25,000 is used in one embodiment of this invention.Smaller step sizes are also possible. It should be obvious that theoptimum selection of the motorized stage 14 and the stage controller 22depends on many factors, including the nature of the sample 12, thedesired time for sample digitization, and the desired resolution of theresulting digital image of the sample 12.

The microscope objective lens 16 can be any microscope objective lenscommonly available. One of ordinary skill in the art will realize thatthe choice of which objective lens to use will depend on the particularcircumstances. In one embodiment of the present invention, themicroscope objective lens 16 is of the infinity-corrected type.

The sample 12 is illuminated by an illumination system 28 that includesa light source 31 and illumination optics 32. The light source 31 in oneembodiment includes a variable intensity halogen light source with aconcave reflective mirror to maximize light output and a KG-1 filter tosuppress heat. However, the light source 31 could also be any other typeof arc-lamp, laser, light emitting diode (“LED”) or other source oflight. The illumination optics 32 in one embodiment include a standardKöhler illumination system with two conjugate planes that are orthogonalto the optical axis. The illumination optics 32 are representative ofthe bright-field illumination optics that can be found on mostcommercially available compound microscopes sold by companies such asCarl Zeiss, Nikon, Olympus, or Leica. One set of conjugate planesincludes (i) a field iris aperture illuminated by the light source 31,(ii) the object plane that is defined by the focal plane of the sample12, and (iii) the plane containing the light-responsive elements of theline scan camera 18. A second conjugate plane includes (i) the filamentof the bulb that is part of the light source 31, (ii) the aperture of acondenser iris that sits immediately before the condenser optics thatare part of the illumination optics 32, and (iii) the back focal planeof the microscope objective lens 16. In one embodiment, the sample 12 isilluminated and imaged in transmission mode, with the line scan camera18 sensing optical energy that is transmitted by the sample 12, orconversely, optical energy that is absorbed by the sample 12.

The scanner 11 of the present invention is equally suitable fordetecting optical energy that is reflected from the sample 12, in whichcase the light source 31, the illumination optics 32, and the microscopeobjective lens 16 must be selected based on compatibility withreflection imaging. One possible embodiment may therefore beillumination through a fiber optic bundle that is positioned above thesample 12. Other possibilities include excitation that is spectrallyconditioned by a monochromator. If the microscope objective lens 16 isselected to be compatible with phase-contrast microscopy, then theincorporation of at least one phase stop in the condenser optics thatare part of the illumination optics 32 will enable the scanner 11 to beused for phase contrast microscopy. To one of ordinary skill in the art,the modifications required for other types of microscopy such asdifferential interference contrast and confocal microscopy should bereadily apparent. Overall, the scanner 11 is suitable, with appropriatebut well-known modifications, for the interrogation of microscopicsamples in any known mode of optical microscopy.

Between the microscope objective lens 16 and the line scan camera 18 aresituated the line scan camera focusing optics 34 that focus the opticalsignal captured by the microscope objective lens 16 onto thelight-responsive elements of the line scan camera 18. In a moderninfinity-corrected microscope the focusing optics between the microscopeobjective lens and the eyepiece optics, or between the microscopeobjective lens and an external imaging port, consist of an opticalelement known as a tube lens that is part of a microscope's observationtube. Many times the tube lens consists of multiple optical elements toprevent the introduction of coma or astigmatism. One of the motivationsfor the relatively recent change from traditional finite tube lengthoptics to infinity corrected optics was to increase the physical spacein which the optical energy from the sample 12 is parallel, meaning thatthe focal point of this optical energy is at infinity. In this case,accessory elements like dichroic mirrors or filters can be inserted intothe infinity space without changing the optical path magnification orintroducing undesirable optical artifacts.

Infinity-corrected microscope objective lenses are typically inscribedwith an infinity mark. The magnification of an infinity correctedmicroscope objective lens is given by the quotient of the focal lengthof the tube lens divided by the focal length of the objective lens. Forexample, a tube lens with a focal length of 180 millimeters will resultin 20× magnification if an objective lens with 9 millimeter focal lengthis used. One of the reasons that the objective lenses manufactured bydifferent microscope manufacturers are not compatible is because of alack of standardization in the tube lens focal length. For example, a20× objective lens from Olympus, a company that uses a 180 millimetertube lens focal length, will not provide a 20× magnification on a Nikonmicroscope that is based on a different tube length focal length of 200millimeters. Instead, the effective magnification of such an Olympusobjective lens engraved with 20× and having a 9 millimeter focal lengthwill be 22.2×, obtained by dividing the 200 millimeter tube lens focallength by the 9 millimeter focal length of the objective lens. Changingthe tube lens on a conventional microscope is virtually impossiblewithout disassembling the microscope. The tube lens is part of acritical fixed element of the microscope. Another contributing factor tothe incompatibility between the objective lenses and microscopesmanufactured by different manufacturers is the design of the eyepieceoptics, the binoculars through which the specimen is observed. Whilemost of the optical corrections have been designed into the microscopeobjective lens, most microscope users remain convinced that there issome benefit in matching one manufacturers' binocular optics with thatsame manufacturers' microscope objective lenses to achieve the bestvisual image.

The line scan camera focusing optics 34 include a tube lens opticmounted inside of a mechanical tube. Since the scanner 11, in oneembodiment, lacks binoculars or eyepieces for traditional visualobservation, the problem suffered by conventional microscopes ofpotential incompatibility between objective lenses and binoculars isimmediately eliminated. One of ordinary skill will similarly realizethat the problem of achieving parfocality between the eyepieces of themicroscope and a digital image on a display monitor is also eliminatedby virtue of not having any eyepieces. Since the scanner 11 alsoovercomes the field of view limitation of a traditional microscope byproviding a field of view that is practically limited only by thephysical boundaries of the sample 12, the importance of magnification inan all-digital imaging microscope such as provided by the presentscanner 11 is limited. Once a portion of the sample 12 has beendigitized, it is straightforward to apply electronic magnification,sometimes known as electric zoom, to an image of the sample 12 in orderto increase its magnification. Increasing the magnification of an imageelectronically has the effect of increasing the size of that image onthe monitor that is used to display the image. If too much electroniczoom is applied, then the display monitor will be able to show onlyportions of the magnified image. It is not possible, however, to useelectronic magnification to display information that was not present inthe original optical signal that was digitized in the first place. Sinceone of the objectives of the scanner 11 is to provide high qualitydigital images, in lieu of visual observation through the eyepieces of amicroscope, it is important that the content of the images acquired bythe scanner 11 include as much image detail as possible. The termresolution is typically used to describe such image detail and the termdiffraction-limited is used to describe the wavelength-limited maximumspatial detail available in an optical signal. The scanner 11 providesdiffraction-limited digital imaging by selection of a tube lens focallength that is matched according to the well know Nyquist samplingcriteria to both the size of an individual pixel element in alight-sensing camera such as the line scan camera 18 and to thenumerical aperture of the microscope objective lens 16. It is well knownthat numerical aperture, not magnification, is the resolution-limitingattribute of a microscope objective lens 16.

An example will help to illustrate the optimum selection of a tube lensfocal length that is part of the line scan camera focusing optics 34.Consider again the 20× microscope objective lens 16 with 9 millimeterfocal length discussed previously and assume that this objective lenshas a numerical aperture of 0.50. Assuming no appreciable degradationfrom the condenser, the diffraction-limited resolving power of thisobjective lens at a wavelength of 500 nanometers is approximately 0.6micrometers, obtained using the well-known Abbe relationship. Assumefurther that the line scan camera 18, which in one embodiment has aplurality of 14 micrometer square pixels, is used to detect a portion ofthe sample 12. In accordance with sampling theory, it is necessary thatat least two sensor pixels subtend the smallest resolvable spatialfeature. In this case, the tube lens must be selected to achieve amagnification of 46.7, obtained by dividing 28 micrometers, whichcorresponds to two 14 micrometer pixels, by 0.6 micrometers, thesmallest resolvable feature dimension. The optimum tube lens optic focallength is therefore about 420 millimeters, obtained by multiplying 46.7by 9. The line scan focusing optics 34 with a tube lens optic having afocal length of 420 millimeters will therefore be capable of acquiringimages with the best possible spatial resolution, similar to what wouldbe observed by viewing a specimen under a microscope using the same 20×objective lens. To reiterate, the scanner 11 utilizes a traditional 20×microscope objective lens 16 in a higher magnification opticalconfiguration, in this example about 47×, in order to acquirediffraction-limited digital images. If a traditional 20× magnificationobjective lens 16 with a higher numerical aperture were used, say 0.75,the required tube lens optic magnification for diffraction-limitedimaging would be about 615 millimeters, corresponding to an overalloptical magnification of 68×. Similarly, if the numerical aperture ofthe 20× objective lens were only 0.3, the optimum tube lens opticmagnification would only be about 28×, which corresponds to a tube lensoptic focal length of approximately 252 millimeters. The line scancamera focusing optics 34 are modular elements of the scanner 11 and canbe interchanged as necessary for optimum digital imaging. The advantageof diffraction-limited digital imaging is particularly significant forapplications, for example bright field microscopy, in which thereduction in signal brightness that accompanies increases inmagnification is readily compensated by increasing the intensity of anappropriately designed illumination system 28.

In principle, it is possible to attach external magnification-increasingoptics to a conventional microscope-based digital imaging system toeffectively increase the tube lens magnification so as to achievediffraction-limited imaging as has just been described for the presentscanner 11; however, the resulting decrease in the field of view isoften unacceptable, making this approach impractical. Furthermore, manyusers of microscopes typically do not understand enough about thedetails of diffraction-limited imaging to effectively employ thesetechniques on their own. In practice, digital cameras are attached tomicroscope ports with magnification-decreasing optical couplers toattempt to increase the size of the field of view to something moresimilar to what can be seen through the eyepiece. The standard practiceof adding de-magnifying optics is a step in the wrong direction if thegoal is to obtain diffraction-limited digital images.

In a conventional microscope, different power objectives lenses aretypically used to view the specimen at different resolutions andmagnifications. Standard microscopes have a nosepiece that holds fiveobjectives lenses. In an all-digital imaging system such as the presentscanner 11 there is a need for only one microscope objective lens 16with a numerical aperture corresponding to the highest spatialresolution desirable. One embodiment of the scanner 11 provides for onlyone microscope objective lens 16. Once a diffraction-limited digitalimage has been captured at this resolution, it is straightforward usingstandard digital image processing techniques, to present imageryinformation at any desirable reduced resolutions and magnifications.

One embodiment of the scanner 11 is based on a Dalsa SPARK line scancamera 18 with 1024 pixels (picture elements) arranged in a lineararray, with each pixel having a dimension of 14 by 14 micrometers. Anyother type of linear array, whether packaged as part of a camera orcustom-integrated into an imaging electronic module, can also be used.The linear array in one embodiment effectively provides eight bits ofquantization, but other arrays providing higher or lower level ofquantization may also be used. Alternate arrays based on 3-channelred-green-blue (RGB) color information or time delay integration (TDI),may also be used. TDI arrays provide a substantially bettersignal-to-noise ratio (SNR) in the output signal by summing intensitydata from previously imaged regions of a specimen, yielding an increasein the SNR that is in proportion to the square-root of the number ofintegration stages. TDI arrays can comprise multiple stages of lineararrays. TDI arrays are available with 24, 32, 48, 64, 96, or even morestages. The scanner 11 also supports linear arrays that are manufacturedin a variety of formats including some with 512 pixels, some with 1024pixels, and others having as many as 4096 pixels. Appropriate, but wellknown, modifications to the illumination system 28 and the line scancamera focusing optics 34 may be required to accommodate larger arrays.Linear arrays with a variety of pixel sizes can also be used in scanner11. The salient requirement for the selection of any type of line scancamera 18 is that the sample 12 can be in motion with respect to theline scan camera 18 during the digitization of the sample 12 in order toobtain high quality images, overcoming the static requirements of theconventional imaging tiling approaches known in the prior art.

The output signal of the line scan camera 18 is connected to the dataprocessor 21. The data processor 21 in one embodiment includes a centralprocessing unit with ancillary electronics, for example a motherboard,to support at least one signal digitizing electronics board such as animaging board or a frame grabber. In the presently embodiment, theimaging board is an EPIX PIXCID24 PCI bus imaging board, however, thereare many other types of imaging boards or frame grabbers from a varietyof manufacturers which could be used in place of the EPIX board. Analternate embodiment could be a line scan camera that uses an interfacesuch as IEEE 1394, also known as Firewire, to bypass the imaging boardaltogether and store data directly on a data storage 38, such as a harddisk.

The data processor 21 is also connected to a memory 36, such as randomaccess memory (RAM), for the short-term storage of data, and to the datastorage 38, such as a hard drive, for long-term data storage. Further,the data processor 21 is connected to a communications port 40 that isconnected to a network 42 such as a local area network (LAN), a widearea network (WAN), a metropolitan area network (MAN), an intranet, anextranet, or the global Internet. The memory 36 and the data storage 38are also connected to each other. The data processor 21 is also capableof executing computer programs, in the form of software, to controlcritical elements of the scanner 11 such as the line scan camera 18 andthe stage controller 22, or for a variety of image-processing functions,image-analysis functions, or networking. The data processor 21 can bebased on any operating system, including operating systems such asWindows, Linux, OS/2, Mac OS, and Unix. In one embodiment, the dataprocessor 21 operates based on the Windows NT operating system.

The data processor 21, memory 36, data storage 38, and communicationport 40 are each elements that can be found in a conventional computer.One example would be a personal computer such as a Dell Dimension XPST500 that features a Pentium III 500 MHz processor and up to 756megabytes (MB) of RAM. In one embodiment, the computer, elements whichinclude the data processor 21, memory 36, data storage 38, andcommunications port 40 are all internal to the scanner 11, so that theonly connection of the scanner 11 to the other elements of the system 10is the communication port 40. In an alternate embodiment of the scanner11, the computer elements would be external to the scanner 11 with acorresponding connection between the computer elements and the scanner11.

The scanner 11, in one embodiment of the invention, integrates opticalmicroscopy, digital imaging, motorized sample positioning, computing,and network-based communications into a single-enclosure unit. The majoradvantage of packaging the scanner 11 as a single-enclosure unit withthe communications port 40 as the primary means of data input and outputare reduced complexity and increased reliability. The various elementsof the scanner 11 are optimized to work together, in sharp contrast totraditional microscope-based imaging systems in which the microscope,light source, motorized stage, camera, and computer are typicallyprovided by different vendors and require substantial integration andmaintenance.

The communication port 40 provides a means for rapid communications withthe other elements of the system 10, including the network 42. Onecommunications protocol for the communications port 40 is acarrier-sense multiple-access collision detection protocol such asEthernet, together with the TCP/IP protocol for transmission control andinternetworking. The scanner 11 is intended to work with any type oftransmission media, including broadband, baseband, coaxial cable,twisted pair, fiber optics, DSL or wireless.

In one embodiment, control of the scanner 11 and review of the imagerydata captured by the scanner 11 are performed on a computer 44 that isconnected to the network 42. The computer 44, in one embodiment, isconnected to a display monitor 46 to provide imagery information to anoperator. A plurality of computers 44 may be connected to the network42. In one embodiment, the computer 44 communicates with the scanner 11using a network browser such as Internet Explorer from Microsoft orNetscape Communicator from AOL. Images are stored on the scanner 11 in acommon compressed format such a JPEG which is an image format that iscompatible with standard image-decompression methods that are alreadybuilt into most commercial browsers. Other standard or non-standard,lossy or lossless, image compression formats will also work. In oneembodiment, the scanner 11 is a webserver providing an operatorinterface that is based on webpages that are sent from the scanner 11 tothe computer 44. For dynamic review of imagery data, one embodiment ofthe scanner 11 is based on playing back, for review on the displaymonitor 46 that is connected to the computer 44, multiple frames ofimagery data using standard multiple-frame browser compatible softwarepackages such as Media-Player from Microsoft, Quicktime from AppleComputer, or RealPlayer from Real Networks. In one embodiment, thebrowser on the computer 44 uses the hypertext transmission protocol(http) together with TCP for transmission control.

There are, and will be in the future, many different means and protocolsby which the scanner 11 could communicate with the computer 44, or aplurality of computers. While one embodiment is based on standard meansand protocols, the approach of developing one or multiple customizedsoftware modules known as applets is equally feasible and may bedesirable for selected future applications of the scanner 11. Further,there are no constraints that computer 44 be of any specific type suchas a personal computer (PC) or be manufactured by any specific companysuch as Dell. One of the advantages of a standardized communicationsport 40 is that any type of computer 44 operating common network browsersoftware can communicate with the scanner 11.

If one so desires, it is possible, with some modifications to thescanner 11, to obtain spectrally resolved images. Spectrally resolvedimages are images in which spectral information is measured at everyimage pixel. Spectrally resolved images could be obtained by replacingthe line scan camera 18 of the scanner 11 with an optical slit and animaging spectrograph. The imaging spectrograph uses a two-dimensionalCCD detector to capture wavelength-specific intensity data for a columnof image pixels by using a prism or grating to disperse the opticalsignal that is focused on the optical slit along each of the rows of thedetector.

Turning now to FIG. 12B, a block diagram of a second embodiment of anoptical microscopy system 10 according to the present invention isshown. In this system 10, the scanner 11 is more complex and expensivethan the embodiment shown in FIG. 12A. The additional attributes of thescanner 11 that are shown do not all have to be present for anyalternate embodiment to function correctly. FIG. 2 is intended toprovide a reasonable example of additional features and capabilitiesthat could be incorporated into the scanner 11.

The alternate embodiment of FIG. 12B provides for a much greater levelof automation than the embodiment of FIG. 12A. A more complete level ofautomation of the illumination system 28 is achieved by connectionsbetween the data processor 21 and both the light source 31 and theillumination optics 32 of the illumination system 28. The connection tothe light source 31 may control the voltage, or current, in an open orclosed loop fashion, in order to control the intensity of the lightsource 31. Recall that the light source 31 is a halogen bulb in oneembodiment. The connection between the data processor 21 and theillumination optics 32 could provide closed loop control of the fieldiris aperture and the condenser iris to provide a means for ensuringthat optimum Köhler illumination is maintained.

Use of the scanner 11 for fluorescence imaging requires easilyrecognized modifications to the light source 31, the illumination optics32, and the microscope objective lens 16. The second embodiment of FIG.12B also provides for a fluorescence filter cube 50 that includes anexcitation filter, a dichroic filter, and a barrier filter. Thefluorescence filter cube 50 is positioned in the infinity corrected beampath that exists between the microscope objective lens 16 and line scancamera focusing optics 34. One embodiment for fluorescence imaging couldinclude the addition of a filter wheel or tunable filter into theillumination optics 32 to provide appropriate spectral excitation forthe variety of fluorescent dyes or nano-crystals available on themarket.

The addition of at least one beam splitter 52 into the imaging pathallows the optical signal to be split into at least two paths. Theprimary path is via the line scan camera focusing optics 34, asdiscussed previously, to enable diffraction-limited imaging by the linescan camera 18. A second path is provided via an area scan camerafocusing optics 54 for imaging by an area scan camera 56. It should bereadily apparent that proper selection of these two focusing optics canensure diffraction-limited imaging by the two camera sensors havingdifferent pixel sizes. The area scan camera 56 can be one of many typesthat are currently available, including a simple color video camera, ahigh performance, cooled, CCD camera, or a variable integration-timefast frame camera. The area scan camera 56 provides a traditionalimaging system configuration for the scanner 11. The area scan camera 56is connected to the data processor 21. If two cameras are used, forexample the line scan camera 18 and the area scan camera 56, both cameratypes could be connected to the data processor using either a singledual-purpose imaging board, two different imaging boards, or theIEEE1394 Firewire interface, in which case one or both imaging boardsmay not be needed. Other related methods of interfacing imaging sensorsto the data processor 21 are also available.

While the primary interface of the scanner 11 to the computer 44 is viathe network 42, there may be instances, for example a failure of thenetwork 42, where it is beneficial to be able to connect the scanner 11directly to a local output device such as a display monitor 58 and toalso provide local input devices such as a keyboard and mouse 60 thatare connected directly into the data processor 21 of the scanner 11. Inthis instance, the appropriate driver software and hardware would haveto be provided as well.

The second embodiment shown in FIG. 12B also provides for a much greaterlevel of automated imaging performance. Enhanced automation of theimaging of the scanner 11 can be achieved by closing the focus controlloop comprising the piezo positioner 24, the piezo controller 26, andthe data processor 21 using well-known methods of autofocus. The secondembodiment also provides for a motorized nose-piece 62 to accommodateseveral objectives lenses. The motorized nose-piece 62 is connected toand directed by the data processor 21 through a nose-piece controller64.

There are other features and capabilities of the scanner 11 which couldbe incorporated. For example, the process of scanning the sample 12 withrespect to the microscope objective lens 16 that is substantiallystationary in the x/y plane of the sample 12 could be modified tocomprise scanning of the microscope objective lens 16 with respect to astationary sample 12. Scanning the sample 12, or scanning the microscopeobjective lens 16, or scanning both the sample 12 and the microscopeobjective lens 16 simultaneously, are possible embodiments of thescanner 11 which can provide the same large contiguous digital image ofthe sample 12 as discussed previously.

The scanner 11 also provides a general purpose platform for automatingmany types of microscope-based analyses. The illumination system 28could be modified from a traditional halogen lamp or arc-lamp to alaser-based illumination system to permit scanning of the sample 12 withlaser excitation. Modifications, including the incorporation of aphotomultiplier tube or other non-imaging detector, in addition to or inlieu of the line scan camera 18 or the area scan camera 56, could beused to provide a means of detecting the optical signal resulting fromthe interaction of the laser energy with the sample 12.

Turning now to FIG. 12C, the line scan camera field of view 70 comprisesthe region of the sample 12 of FIG. 12A that is imaged by a multitude ofindividual pixel elements 72 that are arranged in a linear fashion intoa linear array 74 as shown in FIG. 12C. The linear array 74 of oneembodiment comprises 1024 of the individual pixel elements 72, with eachof the pixel elements 72 being 14 micrometers square. The physicaldimensions of the linear array 74 of one embodiment are 14.34millimeters by 14 micrometers. Assuming, for purposes of discussion ofthe operation of the scanner 11, that the magnification between thesample 12 and the line scan camera 18 is ten, then the line scan camerafield of view 70 corresponds to a region of the sample 12 that hasdimensions equal to 1.43 millimeters by 1.4 micrometers. Each pixelelement 72 images an area about 1.4 micrometers by 1.4 micrometers.

In one embodiment of the scanner 11, the scanning and digitization isperformed in a direction of travel 84 that alternates between imagestrips. This type of bi-directional scanning provides for a more rapiddigitization process than uni-directional scanning, a method of scanningand digitization which requires the same direction of travel 84 for eachimage strip.

The capabilities of the line scan camera 18 and the focusing sensor 30typically determine whether scanning and focusing can be donebi-directionally or uni-directionally. Uni-directional systems oftencomprise more than one linear array 74, such as a three channel colorarray 86 or a multi-channel TDI array 88 shown in FIG. 12C. The colorarray 86 detects the RGB intensities required for obtaining a colorimage. An alternate embodiment for obtaining color information uses aprism to split the broadband optical signal into the three colorchannels. The TDI array 88 could be used in an alternate embodiment ofthe scanner 11 to provide a means of increasing the effectiveintegration time of the line scan camera 18, while maintaining a fastdata rate, and without significant loss in the signal-to-noise ratio ofthe digital imagery data.

FIG. 13 is a block diagram illustrating an example wired or wirelessprocessor-enabled device 550 that may be used in connection with variousembodiments described herein. For example the system 550 may be used asor in conjunction with the line scanning system as previously described.For example, the system 550 can be used to control the various elementsof the line scanning system. The system 550 can be a conventionalpersonal computer, computer server, personal digital assistant, smartphone, tablet computer, or any other processor enabled device that iscapable of wired or wireless data communication. Other computer systemsand/or architectures may be also used, as will be clear to those skilledin the art.

The system 550 preferably includes one or more processors, such asprocessor 560. Additional processors may be provided, such as anauxiliary processor to manage input/output, an auxiliary processor toperform floating point mathematical operations, a special-purposemicroprocessor having an architecture suitable for fast execution ofsignal processing algorithms (e.g., digital signal processor), a slaveprocessor subordinate to the main processing system (e.g., back-endprocessor), an additional microprocessor or controller for dual ormultiple processor systems, or a coprocessor. Such auxiliary processorsmay be discrete processors or may be integrated with the processor 560.

The processor 560 is preferably connected to a communication bus 555.The communication bus 555 may include a data channel for facilitatinginformation transfer between storage and other peripheral components ofthe system 550. The communication bus 555 further may provide a set ofsignals used for communication with the processor 560, including a databus, address bus, and control bus (not shown). The communication bus 555may comprise any standard or non-standard bus architecture such as, forexample, bus architectures compliant with industry standard architecture(“ISA”), extended industry standard architecture (“EISA”), Micro ChannelArchitecture (“MCA”), peripheral component interconnect (“PCI”) localbus, or standards promulgated by the Institute of Electrical andElectronics Engineers (“IEEE”) including IEEE 488 general-purposeinterface bus (“GPIB”), IEEE 696/S-100, and the like.

System 550 preferably includes a main memory 565 and may also include asecondary memory 570. The main memory 565 provides storage ofinstructions and data for programs executing on the processor 560. Themain memory 565 is typically semiconductor-based memory such as dynamicrandom access memory (“DRAM”) and/or static random access memory(“SRAM”). Other semiconductor-based memory types include, for example,synchronous dynamic random access memory (“SDRAM”), Rambus dynamicrandom access memory (“RDRAM”), ferroelectric random access memory(“FRAM”), and the like, including read only memory (“ROM”).

The secondary memory 570 may optionally include a internal memory 575and/or a removable medium 580, for example a floppy disk drive, amagnetic tape drive, a compact disc (“CD”) drive, a digital versatiledisc (“DVD”) drive, etc. The removable medium 580 is read from and/orwritten to in a well-known manner. Removable storage medium 580 may be,for example, a floppy disk, magnetic tape, CD, DVD, SD card, etc.

The removable storage medium 580 is a non-transitory computer readablemedium having stored thereon computer executable code (i.e., software)and/or data. The computer software or data stored on the removablestorage medium 580 is read into the system 550 for execution by theprocessor 560.

In alternative embodiments, secondary memory 570 may include othersimilar means for allowing computer programs or other data orinstructions to be loaded into the system 550. Such means may include,for example, an external storage medium 595 and an interface 570.Examples of external storage medium 595 may include an external harddisk drive or an external optical drive, or and external magneto-opticaldrive.

Other examples of secondary memory 570 may include semiconductor-basedmemory such as programmable read-only memory (“PROM”), erasableprogrammable read-only memory (“EPROM”), electrically erasable read-onlymemory (“EEPROM”), or flash memory (block oriented memory similar toEEPROM). Also included are any other removable storage media 580 andcommunication interface 590, which allow software and data to betransferred from an external medium 595 to the system 550.

System 550 may also include a communication interface 590. Thecommunication interface 590 allows software and data to be transferredbetween system 550 and external devices (e.g. printers), networks, orinformation sources. For example, computer software or executable codemay be transferred to system 550 from a network server via communicationinterface 590. Examples of communication interface 590 include a modem,a network interface card (“NIC”), a wireless data card, a communicationsport, a PCMCIA slot and card, an infrared interface, and an IEEE 1394fire-wire, just to name a few.

Communication interface 590 preferably implements industry promulgatedprotocol standards, such as Ethernet IEEE 802 standards, Fiber Channel,digital subscriber line (“DSL”), asynchronous digital subscriber line(“ADSL”), frame relay, asynchronous transfer mode (“ATM”), integrateddigital services network (“ISDN”), personal communications services(“PCS”), transmission control protocol/Internet protocol (“TCP/IP”),serial line Internet protocol/point to point protocol (“SLIP/PPP”), andso on, but may also implement customized or non-standard interfaceprotocols as well.

Software and data transferred via communication interface 590 aregenerally in the form of electrical communication signals 605. Thesesignals 605 are preferably provided to communication interface 590 via acommunication channel 600. In one embodiment, the communication channel600 may be a wired or wireless network, or any variety of othercommunication links. Communication channel 600 carries signals 605 andcan be implemented using a variety of wired or wireless communicationmeans including wire or cable, fiber optics, conventional phone line,cellular phone link, wireless data communication link, radio frequency(“RF”) link, or infrared link, just to name a few.

Computer executable code (i.e., computer programs or software) is storedin the main memory 565 and/or the secondary memory 570. Computerprograms can also be received via communication interface 590 and storedin the main memory 565 and/or the secondary memory 570. Such computerprograms, when executed, enable the system 550 to perform the variousfunctions of the present invention as previously described.

In this description, the term “computer readable medium” is used torefer to any non-transitory computer readable storage media used toprovide computer executable code (e.g., software and computer programs)to the system 550. Examples of these media include main memory 565,secondary memory 570 (including internal memory 575, removable medium580, and external storage medium 595), and any peripheral devicecommunicatively coupled with communication interface 590 (including anetwork information server or other network device). Thesenon-transitory computer readable mediums are means for providingexecutable code, programming instructions, and software to the system550.

In an embodiment that is implemented using software, the software may bestored on a computer readable medium and loaded into the system 550 byway of removable medium 580, I/O interface 585, or communicationinterface 590. In such an embodiment, the software is loaded into thesystem 550 in the form of electrical communication signals 605. Thesoftware, when executed by the processor 560, preferably causes theprocessor 560 to perform the inventive features and functions previouslydescribed herein.

The system 550 also includes optional wireless communication componentsthat facilitate wireless communication over a voice and over a datanetwork. The wireless communication components comprise an antennasystem 610, a radio system 615 and a baseband system 620. In the system550, radio frequency (“RF”) signals are transmitted and received overthe air by the antenna system 610 under the management of the radiosystem 615.

In one embodiment, the antenna system 610 may comprise one or moreantennae and one or more multiplexors (not shown) that perform aswitching function to provide the antenna system 610 with transmit andreceive signal paths. In the receive path, received RF signals can becoupled from a multiplexor to a low noise amplifier (not shown) thatamplifies the received RF signal and sends the amplified signal to theradio system 615.

In alternative embodiments, the radio system 615 may comprise one ormore radios that are configured to communicate over various frequencies.In one embodiment, the radio system 615 may combine a demodulator (notshown) and modulator (not shown) in one integrated circuit (“IC”). Thedemodulator and modulator can also be separate components. In theincoming path, the demodulator strips away the RF carrier signal leavinga baseband receive audio signal, which is sent from the radio system 615to the baseband system 620.

If the received signal contains audio information, then baseband system620 decodes the signal and converts it to an analog signal. Then thesignal is amplified and sent to a speaker. The baseband system 620 alsoreceives analog audio signals from a microphone. These analog audiosignals are converted to digital signals and encoded by the basebandsystem 620. The baseband system 620 also codes the digital signals fortransmission and generates a baseband transmit audio signal that isrouted to the modulator portion of the radio system 615. The modulatormixes the baseband transmit audio signal with an RF carrier signalgenerating an RF transmit signal that is routed to the antenna systemand may pass through a power amplifier (not shown). The power amplifieramplifies the RF transmit signal and routes it to the antenna system 610where the signal is switched to the antenna port for transmission.

The baseband system 620 is also communicatively coupled with theprocessor 560. The central processing unit 560 has access to datastorage areas 565 and 570. The central processing unit 560 is preferablyconfigured to execute instructions (i.e., computer programs or software)that can be stored in the memory 565 or the secondary memory 570.Computer programs can also be received from the baseband processor 610and stored in the data storage area 565 or in secondary memory 570, orexecuted upon receipt. Such computer programs, when executed, enable thesystem 550 to perform the various functions of the present invention aspreviously described. For example, data storage areas 565 may includevarious software modules (not shown) that were previously described.

Various embodiments may also be implemented primarily in hardware using,for example, components such as application specific integrated circuits(“ASICs”), or field programmable gate arrays (“FPGAs”). Implementationof a hardware state machine capable of performing the functionsdescribed herein will also be apparent to those skilled in the relevantart. Various embodiments may also be implemented using a combination ofboth hardware and software.

Furthermore, those of skill in the art will appreciate that the variousillustrative logical blocks, modules, circuits, and method stepsdescribed in connection with the above described FIGS. and theembodiments disclosed herein can often be implemented as electronichardware, computer software, or combinations of both. To clearlyillustrate this interchangeability of hardware and software, variousillustrative components, blocks, modules, circuits, and steps have beendescribed above generally in terms of their functionality. Whether suchfunctionality is implemented as hardware or software depends upon theparticular application and design constraints imposed on the overallsystem. Skilled persons can implement the described functionality invarying ways for each particular application, but such implementationdecisions should not be interpreted as causing a departure from thescope of the invention. In addition, the grouping of functions within amodule, block, circuit or step is for ease of description. Specificfunctions or steps can be moved from one module, block or circuit toanother without departing from the invention.

Moreover, the various illustrative logical blocks, modules, and methodsdescribed in connection with the embodiments disclosed herein can beimplemented or performed with a general purpose processor, a digitalsignal processor (“DSP”), an ASIC, FPGA or other programmable logicdevice, discrete gate or transistor logic, discrete hardware components,or any combination thereof designed to perform the functions describedherein. A general-purpose processor can be a microprocessor, but in thealternative, the processor can be any processor, controller,microcontroller, or state machine. A processor can also be implementedas a combination of computing devices, for example, a combination of aDSP and a microprocessor, a plurality of microprocessors, one or moremicroprocessors in conjunction with a DSP core, or any other suchconfiguration.

Additionally, the steps of a method or algorithm described in connectionwith the embodiments disclosed herein can be embodied directly inhardware, in a software module executed by a processor, or in acombination of the two. A software module can reside in RAM memory,flash memory, ROM memory, EPROM memory, EEPROM memory, registers, harddisk, a removable disk, a CD-ROM, or any other form of storage mediumincluding a network storage medium. An exemplary storage medium can becoupled to the processor such the processor can read information from,and write information to, the storage medium. In the alternative, thestorage medium can be integral to the processor. The processor and thestorage medium can also reside in an ASIC.

The above description of the disclosed embodiments is provided to enableany person skilled in the art to make or use the invention. Variousmodifications to these embodiments will be readily apparent to thoseskilled in the art, and the generic principles described herein can beapplied to other embodiments without departing from the spirit or scopeof the invention. Thus, it is to be understood that the description anddrawings presented herein represent a presently preferred embodiment ofthe invention and are therefore representative of the subject matterwhich is broadly contemplated by the present invention. It is furtherunderstood that the scope of the present invention fully encompassesother embodiments that may become obvious to those skilled in the artand that the scope of the present invention is accordingly not limited.

What is claimed is:
 1. A system for capturing a digital image of amicroscope slide, the system comprising: an objective lens having anoptical field of view; at least one imaging line sensor positioned in afirst optical path of the optical field of view and configured toreceive light from at least a first portion of the optical field ofview; at least one focusing line sensor positioned in a second opticalpath of the optical field of view and configured to receive light fromat least a second portion of the optical field of view, wherein the atleast one focusing line sensor is tilted at an angle θ with respect toan axis that is perpendicular to the second optical path; and at leastone processor configured to determine a focus height Z at which toposition the objective lens, before imaging the first portion of theoptical field of view using the at least one imaging line sensor, basedon the following relationship:${L = \frac{Z*M_{focusing}^{2}}{\sin\;\theta}},$ wherein L is a locationon the at least one focusing line sensor, and wherein M_(focusing) is anoptical magnification of the second optical path.
 2. The system of claim1, wherein the at least one processor is further configured to controlmovement of the objective lens to position the objective lens, based onthe determined focus height Z, when imaging the light from the firstportion of the optical field of view.
 3. The system of claim 2, whereinthe at least one processor is configured to, during a single scan in onedirection, for each of a plurality of positions on the microscope slide:acquire image data of the position using the at least one focusing linesensor; determine a location L₂ on the at least one focusing line sensorthat has a best focus in the image data acquired using the at least onefocusing line sensor; determine a focus height Z₂ that corresponds tothe location L₂; move the objective lens to the focus height Z₂; andacquire image data of the position using the at least one imaging linesensor while the objective lens is at the focus height Z₂.
 4. The systemof claim 3, wherein determining the focus height Z₂ comprisescalculating the focus height Z₂ as:Z ₂ =Z ₁+(L ₂ −L ₁)*M _(focusing) ², wherein L₁ is a preceding locationon the at least one focusing line sensor, having a best focus in theimage data acquired using the at least one focusing line sensor, for apreceding position on the microscope slide, and wherein Z₁ is a focusheight calculated for L₁.
 5. The system of claim 3, wherein the bestfocus comprises a highest contrast.
 6. The system of claim 1, wherein,while the at least one imaging sensor acquires an image of the lightfrom the first portion of the optical field of view, the at least onefocusing sensor simultaneously acquires an image of the light from thesecond portion of the optical field of view.
 7. The system of claim 6,wherein the first portion of the optical field of view follows thesecond portion of the optical field of view in a scanning direction. 8.The system of claim 7, wherein the first portion of the optical field ofview is in a center of the optical field of view, and wherein the secondportion of the optical field of view is offset from the center of theoptical field of view.
 9. The system of claim 8, wherein the secondportion of the optical field of view is spaced apart from the firstportion of the optical field of view by a distance that is equal to Nscan lines, wherein N is greater than or equal to one.
 10. The system ofclaim 1, further comprising a beam splitter that splits an optical paththrough the objective lens into the first optical path and the secondoptical path.
 11. The system of claim 10, further comprising a mirrorthat bends light within at least one of the first optical path and thesecond optical path.
 12. The system of claim 1, further comprising amicrolens array positioned within the second optical path, such that aplurality of micro images of the first portion of the optical field ofview are formed on each location L on the at least one focusing linesensor.
 13. A method for capturing a digital image of a microscopeslide, comprising: by at least one processor, calculating a focus heightZ at which to position an objective lens, before imaging at least afirst portion of an optical field of view of the objective lens using atleast one imaging line sensor positioned in a first optical path of theoptical field of view, based on the following relationship:${L = \frac{Z*M_{focusing}^{2}}{\sin\;\theta}},$ wherein L is a locationon the at least one focusing line sensor having a best focus value, andwherein M_(focusing) is an optical magnification of the second opticalpath.